A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401009



Internal ID22458879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16149891..16150219hg38UCSC Ensembl
chr21:17522211..17522539hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956152
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401009
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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